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FDA 510(k)

JUNCTIONAL EMERGENCY TREATMENT TOOL MODEL 30-0088

K-Number: K123194 · 2013-01-03

ApplicantNorth American Rescue Products, Inc.
Decision Date2013-01-03
Product CodeDXC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

JUNCTIONAL EMERGENCY TREATMENT TOOL MODEL 30-0088 is the device name listed in this FDA 510(k) record. The listed applicant is North American Rescue Products, Inc.. It received FDA 510(k) clearance on 2013-01-03 under 510(k) number K123194. The device is classified under product code DXC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JUNCTIONAL EMERGENCY TREATMENT TOOL MODEL 30-0088?

JUNCTIONAL EMERGENCY TREATMENT TOOL MODEL 30-0088 is a medical device that received FDA 510(k) clearance on 2013-01-03. The listed applicant is North American Rescue Products, Inc.. The 510(k) number is K123194.

When did JUNCTIONAL EMERGENCY TREATMENT TOOL MODEL 30-0088 receive FDA 510(k) clearance?

JUNCTIONAL EMERGENCY TREATMENT TOOL MODEL 30-0088 received FDA 510(k) clearance on 2013-01-03, under 510(k) number K123194.

Who is the listed applicant for JUNCTIONAL EMERGENCY TREATMENT TOOL MODEL 30-0088?

The FDA 510(k) record lists North American Rescue Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for JUNCTIONAL EMERGENCY TREATMENT TOOL MODEL 30-0088?

The FDA product code for JUNCTIONAL EMERGENCY TREATMENT TOOL MODEL 30-0088 is DXC.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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